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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-Thiophenecarbonitrile, 4-methyl-

Cc1cscc1C#N Request for Quotation
Chemical Name: 3-Thiophenecarbonitrile, 4-methyl-
CAS Number: 73229-39-7
Product Number: AG005PYA(AGN-PC-0NJFA6)
Synonyms:
MDL No:
Molecular Formula: C6H5NS
Molecular Weight: 123.1756

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
123.173g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
123.014g/mol
Monoisotopic Mass:
123.014g/mol
Topological Polar Surface Area:
52A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
124
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Methylthiophene-3-carbonitrile is a versatile chemical compound widely used in chemical synthesis processes. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure and reactivity make it highly valuable for creating diverse molecular structures and functional groups.  By incorporating 4-Methylthiophene-3-carbonitrile into organic reactions, chemists can introduce a nitrile group and a methylthiophene ring simultaneously, allowing for efficient and selective modifications of target molecules. This compound is particularly useful in the synthesis of heterocyclic compounds, which are key components in many biologically active molecules. Additionally, 4-Methylthiophene-3-carbonitrile's presence can impart desirable properties to the final product, such as enhanced stability, increased biological activity, or improved solubility. Its applications extend to fields such as medicinal chemistry, material science, and chemical manufacturing, making it an essential tool for modern chemical research and development.